A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188358



Internal ID20755398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:69180563..69206733hg38UCSC Ensembl
chr14:69647280..69673450hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg3826171
hg1926171
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6490834
Supporting Variants
Samples
Known GenesEXD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188358
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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